(Q72497776)

(4aS,6aS,6bR,8aR,12aR,12bR,14bS)-10-(acetyloxy)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid

1 reference

10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

1 reference

(4aS,6aS,6bR,10S,12aR,14bS)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

1 reference

mass

498.37091008 dalton

1 reference

(4aS,6aS,6aR,6bR,8aR,10S,12aR,14bS)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

stereoisomer of

2 references

inferred from InChIKey

(4aS,6aS,6bR,8aR,10S,12aR,12bS,14bS)-10-(acetyloxy)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid

2 references

inferred from InChIKey

(4aS,6aS,6bR,8aS,10S,12aR,12bS,14bR)-10-(acetyloxy)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid

1 reference

(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

1 reference

(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

1 reference

(4aS,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

1 reference

(4aS,6aR,6aR,6bS,8aR,10S,12aS,14bR)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

1 reference

(4aR,6aR,6aS,6bR,8aR,10R,12aR,14bR)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

1 reference

chemical formula

C₃₂H₅₀O₄

0 references

canonical SMILES

O=C(OC1CCC2(C)C3CC=C4C5CC(C)(C)CCC5(C(=O)O)CCC4(C)C3(C)CCC2C1(C)C)C

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isomeric SMILES

CC(=O)O[C@H]1CC[C@]2([C@H](C1(C)C)CC[C@@]3([C@@H]2CC=C4[C@]3(CC[C@@]5([C@H]4CC(CC5)(C)C)C(=O)O)C)C)C

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found in taxon

Prunus africana

1 reference

Characterization of Pygeum africanum bark extracts by HRGC with computer assistance

Akebia trifoliata

1 reference

Anthocyanins from Akebia and Stauntonia

Acalypha spiciflora

2 references

Clerodanes and other constituents of Cleidion spiciflorum

Clerodanes and other constituents of Cleidion spiciflorum

Diospyros eriantha

2 references

Pharmacology and chemotaxonomy of Diospyros

The constituents of the bark of diospyros maritima bl.

Diospyros lotus

3 references

Pharmacology and chemotaxonomy of Diospyros

Naphthoquinones and triterpenes from some asian Diospyros species

Naphthoquinones and triterpenes from some asian Diospyros species

Drypetes molunduana

2 references

Sesquiterpene lactone and friedelane derivative from drypetes molunduana

Sesquiterpene lactone and friedelane derivative from drypetes molunduana

Eysenhardtia platycarpa

2 references

Antihyperglycemic Activity and Chemical Constituents ofEysenhardtia platycarpa

Antihyperglycemic Activity and Chemical Constituents ofEysenhardtia platycarpa

Helichrysum forskahlii

2 references

Flavonoids and terpenoids from Helichrysum forskahlii

Flavonoids and terpenoids from Helichrysum forskahlii

Lippia origanoides

3 references

Chemical constituents from Lippia sidoides and cytotoxic activity

[Chemical constituents from Pteris multifida and cytotoxic activity].

Chemical constituents from Lippia sidoides and cytotoxic activity

Lippia sidoides

3 references

Chemical constituents from Lippia sidoides and cytotoxic activity

[Chemical constituents from Pteris multifida and cytotoxic activity].

Chemical constituents from Lippia sidoides and cytotoxic activity

Nuxia sphaerocephala

2 references

Clerodane and labdane diterpenoids from Nuxia sphaerocephala

Clerodane and labdane diterpenoids from Nuxia sphaerocephala

Salvia amplexicaulis

2 references

Cardioactive and antibacterial terpenoids from some Salvia species

Cardioactive diterpenoids from the roots of Salvia amplexicaulis

Senecio burtonii

2 references

Secondary metabolites from Senecio burtonii (Compositae)

Secondary metabolites from Senecio burtonii (Compositae)

Sideritis kuegleriana

2 references

A chemotaxonomic study of nine Canarian Sideritis species

A chemotaxonomic study of nine Canarian Sideritis species

Salvia palaestina

1 reference

Modified abietane diterpenoids and a methoxylupane derivative from Salvia palaestina

Diospyros argentea

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Diospyros blancoi

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Diospyros ismailii

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Diospyros maingayi

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Diospyros siamang

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Diospyros singaporensis

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Diospyros sumatrana

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Diospyros wallichii

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Euptelea polyandra

3 references

Constituents of the Bark of Euptelea polyandra

Studies on inhibitors of skin-tumor promotion, I. Inhibitory effects of triterpenes from Euptelea polyandra on Epstein-Barr virus activation

Studies on inhibitors of skin-tumor promotion, I. Inhibitory effects of triterpenes from Euptelea polyandra on Epstein-Barr virus activation

Ilex rotunda

2 references

A dimeric sinapaldehyde glucoside from Ilex rotunda

A dimeric sinapaldehyde glucoside from Ilex rotunda

Mussaenda macrophylla

3 references

Activity of triterpenoid glycosides from the root bark of Mussaenda macrophylla against two oral pathogens

Activity of triterpenoid glycosides from the root bark of Mussaenda macrophylla against two oral pathogens

Activity of triterpenoid glycosides from the root bark of Mussaenda macrophylla against two oral pathogens

Phytolacca bogotensis

1 reference

3-acetyloleanolic acid from Phytolacca americana seeds

Stauntonia hexaphylla

1 reference

The Triterpenes from Stauntonia hexaphylla Callus Tissues and Their Biosynthetic Significance

Syncarpia glomulifera

2 references

Biologically active triterpenoids of Syncarpia glomulifera bark extract from Paluma, north Queensland, Australia

Biologically active triterpenoids of Syncarpia glomulifera bark extract from Paluma, north Queensland, Australia

Ternstroemia gymnanthera

1 reference

Jacaranone and related compounds from the fresh fruits of Ternstroemia japonica and their antioxidative activity

Ternstroemia japonica

1 reference

Jacaranone and related compounds from the fresh fruits of Ternstroemia japonica and their antioxidative activity

Eucalyptus camaldulensis

1 reference

Structure and spasmolytic activity of eucalyptanoic acid from Eucalyptus camaldulensis var. obtusa and synthesis of its active derivative from oleanolic acid

Myrcia guianensis

1 reference

Triterpenoids as novel natural inhibitors of human cathepsin L

Alchornea laxiflora

1 reference

Two New Fatty Acid Derivatives from the Stem Bark of Alchornea laxiflora (Euphorbiaceae)

Anaphalis sinica

1 reference

Chemical Components ofAnaphalis SinicaHance

Asclepias curassavica

1 reference

Cytotoxic principles from the formosan milkweed, Asclepias curassavica

Betula alnoides

1 reference

Triterpenoids from Betula alnoides.

Betula dahurica

2 references

Triterpenoids of the bark and twigs ofBetula dahurica

Chemical Evaluation of Betula Species in Japan. IV. Constituents of Betula davurica.

Betula davurica

1 reference

Chemical Evaluation of Betula Species in Japan. IV. Constituents of Betula davurica.

Betula ermanii

1 reference

Isoprenoids of the outer bark of the Far Eastern birches Betula costata and Betula ermanii

Betula maximowicziana

2 references

Chemical Evaluation of Betula Species in Japan. III. Constituents of Betula maximowicziana.

Triterpenoids of the outer bark ofBetula maximowicziana

Betula pendula

1 reference

Chemical Evaluation of Betula Species in Japan. II. Constituents of Betula platyphylla var. japonica.

Betula platyphylla

1 reference

Chemical Evaluation of Betula Species in Japan. II. Constituents of Betula platyphylla var. japonica.

Calendula officinalis

1 reference

New Triterpenic Esters of Oleanene-Series from the Flowers of Calendula officinalis Linn.

Cistus monspeliensis

1 reference

Antileishmanial activity of natural diterpenes from Cistus sp. and semisynthetic derivatives thereof

Clerodendrum indicum

1 reference

Clerodendrone, a Novel Hydroquinone Diterpenoid from Clerodendrum Indicum

Croton ciliatoglandulifer

1 reference

Nitrogen-containing phorbol esters from Croton ciliatoglandulifer and their effects on cyclooxygenases-1 and -2

Diospyros maritima

1 reference

Chemical constituents from the stems of Diospyros maritima

Guazuma ulmifolia

1 reference

A new biscoumarin and other constituents from Guazuma tomentosa ROOTS

Lantana camara

1 reference

Triterpenoids, essential oil and photo-oxidative 28 --> 13-lactonization of oleanolic acid from Lantana camara

Perovskia atriplicifolia

1 reference

A new acylated steroid glucoside from Perovskia atriplicifolia

Pieris japonica

1 reference

Triterpenoids of the bark of Pieris japonica D. Don.

Salvia recognita

1 reference

Norabietane diterpenoids and other terpenoids from salvia recognita

Scorzonera cretica

1 reference

Three new dihydroisocoumarins from the Greek endemic species Scorzonera cretica

Serjania triquetra

1 reference

Isolation and relay synthesis of 11α-hydroperoxy diacetyl hederagenin, a novel triterpenoid derivative from Serjania triquetra (Sapindaceae). Biogenetic implications.

Strychnos potatorum

1 reference

Studies on the chemical constituents of the seeds of Strychnos potatorum L. Part I

Tripterygium hypoglaucum

1 reference

Triterpenoids from Tripterygium wilfordii

Vitex negundo

1 reference

A furanoeremophilane from Vitex negundo

Tripterygium wilfordii

1 reference

Triterpenoids from Tripterygium wilfordii

Gelasia cretica

1 reference

Three new dihydroisocoumarins from the Greek endemic species Scorzonera cretica

Ligustrum japonicum

1 reference

Chemical constituents from fruits of Ligustrum lucidum

Stauntonia yaoshanensis

1 reference

Anti-HIV-1 protease triterpenoids from Stauntonia obovatifoliola Hayata subsp. intermedia

Rosmarinus officinalis

1 reference

Rofficerone: A New Triterpenoid from Rosmarinus officinalis

Betula dauurica

1 reference

Chemical Evaluation of Betula Species in Japan. IV. Constituents of Betula davurica.

Salvia yangii

1 reference

A new acylated steroid glucoside from Perovskia atriplicifolia

Ligustrum lucidum

1 reference

Chemical constituents from fruits of Ligustrum lucidum

Diospyros blancoi

1 reference

Naphthoquinones and triterpenes from some asian Diospyros species

Delonix regia

1 reference

Isolation and antibacterial activity of oleananoic acid acetate from Delonix regia leaves

Identifiers

InChI

InChI=1S/C32H50O4/c1-20(33)36-25-12-13-29(6)23(28(25,4)5)11-14-31(8)24(29)10-9-21-22-19-27(2,3)15-17-32(22,26(34)35)18-16-30(21,31)7/h9,22-25H,10-19H2,1-8H3,(H,34,35)/t22-,23-,24+,25-,29-,30+,31+,32-/m0/s1

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InChIKey

RIXNFYQZWDGQAE-DFHVBEEKSA-N

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CAS Registry Number

4339-72-4

1 reference

InChIKey

RIXNFYQZWDGQAE-DFHVBEEKSA-N

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=4339-72-4

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1 reference

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DSSTOX compound identifier

DTXCID901390774

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Human Metabolome Database ID

HMDB0302923

1 reference